The Central Drugs Standard Control Organisation (CDSCO) is under Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India and the National Regulatory Authority (NRA) of India. I am disscused here Explore new openings in Pharma profession by making yourself skilled as Technical associate in The Central Drugs Standard Control Organisation (CDSCO)….
Data integrity is key in a pharmaceutical quality system ensuring that products are of the desired quality. Data Integrity is increasingly becoming a critical GMP issue in the Pharmaceutical and Medical Device Industry. ALCOA-plus. A normally used word form for “attributable, legible, contemporaneous, original and accurate” The descriptor ALCOA has been around since the 1990’s ensuring by regulated…
GOWNING PROCEDURE IN CLEAN ROOM Most Popular Articles What is the fumigation and fogging? What is viable and nonviable Particle Count? Scope for Science Graduate & Post Graduate Types of Clean Room Airlocks in cGMP Facility Simplified CAPA with Investigation Tools, Route Cause Analysis & Risk Management KNOW ABOUT TOTAL QUALITY MANAGEMENT AND CURRENT GOOD…
How to Crack Your Job Interview? Today I shall discuss a topic which is very common topic i,e “How to Crack Your Job Interview?” but I can assure you that my experience will reduce the phobia for an interview. First of all, before going for an interview you should decide whether the job option is…
10-Deacetylbaccatins (10 DAB) is a series of closely related natural organic compounds isolated from the yew tree (Genera Taxus). 10-DAB is also isolated from the needles (leaves) and roots of the Canadian Yew tree, Taxus canadensis, the American ornamental Yew Tree, Taxus media “hicksii” or the European Yew Tree, Taxus baccata, utilizing patented Super Fluid…
Difference between C8 and C18 Columns Used in HPLC System About the Author Mr. Riaz Akhtar (Zydus Cadila) C8 and C18 both types of columns are used in pharmaceutical analysis but their use is specific for analysis of different products. Here we are discussing the difference between C18 and C8. High-Performance…
Airlocks: Contamination is a major factor in pharmaceutical industries. Control of contamination is a major issue for regulatory authorities in the past decade and many major steps have been implemented in pharmaceuticals in order to curb contamination. GMP Guidelines are continuously revised and new amendments have been implemented one such amendment to control the contamination…
About Author: Mr. Shoab Malek [email protected] (Certified Quality Auditor) Degree Required:- B.Sc :- Bachelor of Science with subject of Chemistry, Microbiology, Biotechnology & Zoology can work in pharmaceutical, life science, Biologicals & Medical device industry as a Trainee in Production, QC, Micro Or Warehouse Department. Some Clinical Research Organization (CRO) are also hired come B.Sc…
